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Blood donor‐derived buffy coat to produce platelets in vitro
Background and objectives Platelet transfusion is a standard medical therapy used to treat several bleeding disorders. However, a critical drawback is the dependency on donor‐derived platelets, which leads to concerns like insufficient availability and immunological complications. In vitro platelet...
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Published in: | Vox sanguinis 2020-01, Vol.115 (1), p.94-102 |
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creator | Marini, Irene Rigoni, Flavianna Zlamal, Jan Pelzl, Lisann Althaus, Karina Nowak‐Harnau, Stefanie Rondina, Matthew T. Bakchoul, Tamam |
description | Background and objectives
Platelet transfusion is a standard medical therapy used to treat several bleeding disorders. However, a critical drawback is the dependency on donor‐derived platelets, which leads to concerns like insufficient availability and immunological complications. In vitro platelet production from hematopoietic progenitor cells (CD34) may represent a reasonable solution.
Materials and methods
CD34+ cells were isolated from either buffy coat or peripheral blood and compared in terms of platelet production in vitro. The number and the quality of magnetically isolated CD34+ cells and their capability to differentiate into mature megakaryocytes were investigated using flow cytometry. Additionally, the functionality of megakaryocytes in term of in vitro platelet production was tested.
Results
Similar purity and quantity of CD34+ cells was found after their isolation from both cell sources. In contrast, after 6 days of culture, enhanced number of CD34+ cells isolated from buffy coat compared with peripheral blood was observed (5·3 x 106 vs. 3·0 x 106, respectively). Interestingly, despite a comparable nuclear maturation phenotype, the yield of platelets released from buffy coat‐derived megakaryocytes was significantly higher than from peripheral blood cells (platelet yield pro MK: 7·2 vs. 2·7, respectively). Importantly, platelets produced from buffy coat‐derived cells could be activated by agonists.
Conclusion
Haematopoietic progenitor cells isolated from buffy coat have increased yield of platelets released from mature megakaryocytes and enhanced in vitro functionality, compared with peripheral blood‐derived cells. Our study, suggests that buffy coat, obtained during blood donation processing, might be a promising source of megakaryocytes for in vitro platelet production. |
doi_str_mv | 10.1111/vox.12863 |
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Platelet transfusion is a standard medical therapy used to treat several bleeding disorders. However, a critical drawback is the dependency on donor‐derived platelets, which leads to concerns like insufficient availability and immunological complications. In vitro platelet production from hematopoietic progenitor cells (CD34) may represent a reasonable solution.
Materials and methods
CD34+ cells were isolated from either buffy coat or peripheral blood and compared in terms of platelet production in vitro. The number and the quality of magnetically isolated CD34+ cells and their capability to differentiate into mature megakaryocytes were investigated using flow cytometry. Additionally, the functionality of megakaryocytes in term of in vitro platelet production was tested.
Results
Similar purity and quantity of CD34+ cells was found after their isolation from both cell sources. In contrast, after 6 days of culture, enhanced number of CD34+ cells isolated from buffy coat compared with peripheral blood was observed (5·3 x 106 vs. 3·0 x 106, respectively). Interestingly, despite a comparable nuclear maturation phenotype, the yield of platelets released from buffy coat‐derived megakaryocytes was significantly higher than from peripheral blood cells (platelet yield pro MK: 7·2 vs. 2·7, respectively). Importantly, platelets produced from buffy coat‐derived cells could be activated by agonists.
Conclusion
Haematopoietic progenitor cells isolated from buffy coat have increased yield of platelets released from mature megakaryocytes and enhanced in vitro functionality, compared with peripheral blood‐derived cells. Our study, suggests that buffy coat, obtained during blood donation processing, might be a promising source of megakaryocytes for in vitro platelet production.</description><identifier>ISSN: 0042-9007</identifier><identifier>EISSN: 1423-0410</identifier><identifier>DOI: 10.1111/vox.12863</identifier><identifier>PMID: 31709567</identifier><language>eng</language><publisher>England: S. Karger AG</publisher><subject>Bleeding ; Blood & organ donations ; Blood Buffy Coat - cytology ; Blood cells ; Blood Donors ; Blood Platelets ; Buffy coat ; CD34 antigen ; Cell culture ; Cell differentiation ; Coating ; Complications ; Flow Cytometry ; Hematopoiesis ; Hematopoietic stem cells ; Hematopoietic Stem Cells - physiology ; Humans ; Immunology ; Megakaryocytes ; Peripheral blood ; Phenotypes ; platelet generation ; Platelets ; Progenitor cells ; thrombocytopenia ; Transfusion ; Yield</subject><ispartof>Vox sanguinis, 2020-01, Vol.115 (1), p.94-102</ispartof><rights>2019 International Society of Blood Transfusion</rights><rights>2019 International Society of Blood Transfusion.</rights><rights>Copyright Vox Sanguinis © 2020 International Society of Blood Transfusion</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4193-8dd6673cc851ea1696f7ff4da6d2088dd1ba8ffb6b6118c14a9b97ff072f68bb3</citedby><cites>FETCH-LOGICAL-c4193-8dd6673cc851ea1696f7ff4da6d2088dd1ba8ffb6b6118c14a9b97ff072f68bb3</cites><orcidid>0000-0002-6797-6812</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31709567$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marini, Irene</creatorcontrib><creatorcontrib>Rigoni, Flavianna</creatorcontrib><creatorcontrib>Zlamal, Jan</creatorcontrib><creatorcontrib>Pelzl, Lisann</creatorcontrib><creatorcontrib>Althaus, Karina</creatorcontrib><creatorcontrib>Nowak‐Harnau, Stefanie</creatorcontrib><creatorcontrib>Rondina, Matthew T.</creatorcontrib><creatorcontrib>Bakchoul, Tamam</creatorcontrib><title>Blood donor‐derived buffy coat to produce platelets in vitro</title><title>Vox sanguinis</title><addtitle>Vox Sang</addtitle><description>Background and objectives
Platelet transfusion is a standard medical therapy used to treat several bleeding disorders. However, a critical drawback is the dependency on donor‐derived platelets, which leads to concerns like insufficient availability and immunological complications. In vitro platelet production from hematopoietic progenitor cells (CD34) may represent a reasonable solution.
Materials and methods
CD34+ cells were isolated from either buffy coat or peripheral blood and compared in terms of platelet production in vitro. The number and the quality of magnetically isolated CD34+ cells and their capability to differentiate into mature megakaryocytes were investigated using flow cytometry. Additionally, the functionality of megakaryocytes in term of in vitro platelet production was tested.
Results
Similar purity and quantity of CD34+ cells was found after their isolation from both cell sources. In contrast, after 6 days of culture, enhanced number of CD34+ cells isolated from buffy coat compared with peripheral blood was observed (5·3 x 106 vs. 3·0 x 106, respectively). Interestingly, despite a comparable nuclear maturation phenotype, the yield of platelets released from buffy coat‐derived megakaryocytes was significantly higher than from peripheral blood cells (platelet yield pro MK: 7·2 vs. 2·7, respectively). Importantly, platelets produced from buffy coat‐derived cells could be activated by agonists.
Conclusion
Haematopoietic progenitor cells isolated from buffy coat have increased yield of platelets released from mature megakaryocytes and enhanced in vitro functionality, compared with peripheral blood‐derived cells. Our study, suggests that buffy coat, obtained during blood donation processing, might be a promising source of megakaryocytes for in vitro platelet production.</description><subject>Bleeding</subject><subject>Blood & organ donations</subject><subject>Blood Buffy Coat - cytology</subject><subject>Blood cells</subject><subject>Blood Donors</subject><subject>Blood Platelets</subject><subject>Buffy coat</subject><subject>CD34 antigen</subject><subject>Cell culture</subject><subject>Cell differentiation</subject><subject>Coating</subject><subject>Complications</subject><subject>Flow Cytometry</subject><subject>Hematopoiesis</subject><subject>Hematopoietic stem cells</subject><subject>Hematopoietic Stem Cells - physiology</subject><subject>Humans</subject><subject>Immunology</subject><subject>Megakaryocytes</subject><subject>Peripheral blood</subject><subject>Phenotypes</subject><subject>platelet generation</subject><subject>Platelets</subject><subject>Progenitor cells</subject><subject>thrombocytopenia</subject><subject>Transfusion</subject><subject>Yield</subject><issn>0042-9007</issn><issn>1423-0410</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp10LtOwzAUBmALgWgpDLwAisQCQ6gdO46zIEHFTarUBRCb5auUKo2LnRS68Qg8I0-CIYUBCS9n8Kdf5_wAHCJ4huIbr9zrGcoYxVtgiEiGU0gQ3AZDCEmWlhAWA7AXwhxCyDKW74IBRgUsc1oMwfll7ZxOtGuc_3h718ZXK6MT2Vm7TpQTbdK6ZOmd7pRJlrVoTW3akFRNsqpa7_bBjhV1MAebOQIP11f3k9t0Oru5m1xMU0VQiVOmNaUFVorlyAhES2oLa4kWVGeQxV8kBbNWUkkRYgoRUcoyClhkljIp8Qic9LlxlefOhJYvqqBMXYvGuC7wDCNM85zkMNLjP3TuOt_E7aLCJaHx8iKq014p70LwxvKlrxbCrzmC_KtUHkvl36VGe7RJ7OTC6F_502IE4x68VLVZ_5_EH2dPfeQn4IWBIg</recordid><startdate>202001</startdate><enddate>202001</enddate><creator>Marini, Irene</creator><creator>Rigoni, Flavianna</creator><creator>Zlamal, Jan</creator><creator>Pelzl, Lisann</creator><creator>Althaus, Karina</creator><creator>Nowak‐Harnau, Stefanie</creator><creator>Rondina, Matthew T.</creator><creator>Bakchoul, Tamam</creator><general>S. Karger AG</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T5</scope><scope>7TM</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6797-6812</orcidid></search><sort><creationdate>202001</creationdate><title>Blood donor‐derived buffy coat to produce platelets in vitro</title><author>Marini, Irene ; Rigoni, Flavianna ; Zlamal, Jan ; Pelzl, Lisann ; Althaus, Karina ; Nowak‐Harnau, Stefanie ; Rondina, Matthew T. ; Bakchoul, Tamam</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4193-8dd6673cc851ea1696f7ff4da6d2088dd1ba8ffb6b6118c14a9b97ff072f68bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Bleeding</topic><topic>Blood & organ donations</topic><topic>Blood Buffy Coat - cytology</topic><topic>Blood cells</topic><topic>Blood Donors</topic><topic>Blood Platelets</topic><topic>Buffy coat</topic><topic>CD34 antigen</topic><topic>Cell culture</topic><topic>Cell differentiation</topic><topic>Coating</topic><topic>Complications</topic><topic>Flow Cytometry</topic><topic>Hematopoiesis</topic><topic>Hematopoietic stem cells</topic><topic>Hematopoietic Stem Cells - physiology</topic><topic>Humans</topic><topic>Immunology</topic><topic>Megakaryocytes</topic><topic>Peripheral blood</topic><topic>Phenotypes</topic><topic>platelet generation</topic><topic>Platelets</topic><topic>Progenitor cells</topic><topic>thrombocytopenia</topic><topic>Transfusion</topic><topic>Yield</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marini, Irene</creatorcontrib><creatorcontrib>Rigoni, Flavianna</creatorcontrib><creatorcontrib>Zlamal, Jan</creatorcontrib><creatorcontrib>Pelzl, Lisann</creatorcontrib><creatorcontrib>Althaus, Karina</creatorcontrib><creatorcontrib>Nowak‐Harnau, Stefanie</creatorcontrib><creatorcontrib>Rondina, Matthew T.</creatorcontrib><creatorcontrib>Bakchoul, Tamam</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Vox sanguinis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marini, Irene</au><au>Rigoni, Flavianna</au><au>Zlamal, Jan</au><au>Pelzl, Lisann</au><au>Althaus, Karina</au><au>Nowak‐Harnau, Stefanie</au><au>Rondina, Matthew T.</au><au>Bakchoul, Tamam</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Blood donor‐derived buffy coat to produce platelets in vitro</atitle><jtitle>Vox sanguinis</jtitle><addtitle>Vox Sang</addtitle><date>2020-01</date><risdate>2020</risdate><volume>115</volume><issue>1</issue><spage>94</spage><epage>102</epage><pages>94-102</pages><issn>0042-9007</issn><eissn>1423-0410</eissn><abstract>Background and objectives
Platelet transfusion is a standard medical therapy used to treat several bleeding disorders. However, a critical drawback is the dependency on donor‐derived platelets, which leads to concerns like insufficient availability and immunological complications. In vitro platelet production from hematopoietic progenitor cells (CD34) may represent a reasonable solution.
Materials and methods
CD34+ cells were isolated from either buffy coat or peripheral blood and compared in terms of platelet production in vitro. The number and the quality of magnetically isolated CD34+ cells and their capability to differentiate into mature megakaryocytes were investigated using flow cytometry. Additionally, the functionality of megakaryocytes in term of in vitro platelet production was tested.
Results
Similar purity and quantity of CD34+ cells was found after their isolation from both cell sources. In contrast, after 6 days of culture, enhanced number of CD34+ cells isolated from buffy coat compared with peripheral blood was observed (5·3 x 106 vs. 3·0 x 106, respectively). Interestingly, despite a comparable nuclear maturation phenotype, the yield of platelets released from buffy coat‐derived megakaryocytes was significantly higher than from peripheral blood cells (platelet yield pro MK: 7·2 vs. 2·7, respectively). Importantly, platelets produced from buffy coat‐derived cells could be activated by agonists.
Conclusion
Haematopoietic progenitor cells isolated from buffy coat have increased yield of platelets released from mature megakaryocytes and enhanced in vitro functionality, compared with peripheral blood‐derived cells. Our study, suggests that buffy coat, obtained during blood donation processing, might be a promising source of megakaryocytes for in vitro platelet production.</abstract><cop>England</cop><pub>S. Karger AG</pub><pmid>31709567</pmid><doi>10.1111/vox.12863</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-6797-6812</orcidid></addata></record> |
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subjects | Bleeding Blood & organ donations Blood Buffy Coat - cytology Blood cells Blood Donors Blood Platelets Buffy coat CD34 antigen Cell culture Cell differentiation Coating Complications Flow Cytometry Hematopoiesis Hematopoietic stem cells Hematopoietic Stem Cells - physiology Humans Immunology Megakaryocytes Peripheral blood Phenotypes platelet generation Platelets Progenitor cells thrombocytopenia Transfusion Yield |
title | Blood donor‐derived buffy coat to produce platelets in vitro |
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